scholarly journals A Modular Cascade Synthetic Strategy Toward Structurally Constrained Boron‐doped Polycyclic Aromatic Hydrocarbons

2021 ◽  
Author(s):  
Jin-jiang Zhang ◽  
Lin Yang ◽  
Fupin Liu ◽  
Yubin Fu ◽  
Junzhi Liu ◽  
...  
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Aromatic Hydrocarbons ◽  
Synthetic Strategy ◽  
Boron Doped ◽  
Polycyclic Aromatic

scholarly journals One‐Pot Synthesis of Boron‐Doped Polycyclic Aromatic Hydrocarbons via 1,4‐Boron Migration

2020 ◽  
Author(s):  
Jin‐Jiang Zhang ◽  
Man‐Chung Tang ◽  
Yubin Fu ◽  
Kam‐Hung Low ◽  
Ji Ma ◽  
...  
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Aromatic Hydrocarbons ◽  
One Pot ◽  
One Pot Synthesis ◽  
Boron Doped ◽  
Polycyclic Aromatic

Synthesis of Boron-Doped Polycyclic Aromatic Hydrocarbons by Tandem Intramolecular Electrophilic Arene Borylation

2015 ◽  
Vol 17 (24) ◽  
pp. 6158-6161 ◽  
Author(s):  
Fumiya Miyamoto ◽  
Soichiro Nakatsuka ◽  
Keitaro Yamada ◽  
Ken-ichi Nakayama ◽  
Takuji Hatakeyama
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Aromatic Hydrocarbons ◽  
Boron Doped ◽  
Polycyclic Aromatic

A Vicinal Electrophilic Diborylation Reaction Furnishes Doubly Boron-Doped Polycyclic Aromatic Hydrocarbons

2017 ◽  
Vol 129 (20) ◽  
pp. 5680-5684 ◽  
Author(s):  
Alexandra John ◽  
Michael Bolte ◽  
Hans-Wolfram Lerner ◽  
Matthias Wagner
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Aromatic Hydrocarbons ◽  
Boron Doped ◽  
Polycyclic Aromatic

scholarly journals Fully Fused Boron-Doped Polycyclic Aromatic Hydrocarbons: Their Synthesis, Structure–Property Relationships, and Self-Assembly Behavior in Aqueous Media

2022 ◽  
Author(s):  
Hiroki Narita ◽  
Heekyoung Choi ◽  
Masato Ito ◽  
Naoki Ando ◽  
Soichiro Ogi ◽  
...  
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Aromatic Hydrocarbons ◽  
Self Assembly ◽  
Aqueous Media ◽  
Structure Property ◽  
Organic Optoelectronics ◽  
Structure Property Relationships ◽  
Boron Doped ◽  
Polycyclic Aromatic ◽  
Assembly Behavior

Planarized triarylboranes are attracting increasing attention not only as models of boron-doped graphenes, but also as promising materials for organic optoelectronics. In particular, polycyclic aromatic hydrocarbon (PAH) skeletons with embedded...

Cyclic Alkyne Approach to Heteroatom-Containing Polycyclic Aromatic Hydrocarbon Scaffolds

2019 ◽  
Author(s):  
Evan Darzi ◽  
Joyann Barber ◽  
Neil Garg
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Polycyclic Aromatic Hydrocarbon ◽  
Aromatic Hydrocarbon ◽  
Aromatic Hydrocarbons ◽  
Diels Alder ◽  
Pericyclic Reactions ◽  
One Pot ◽  
Synthetic Strategy ◽  
Polycyclic Aromatic

We report a modular synthetic strategy for accessing heteroatom-containing polycyclic aromatic hydrocarbons (PAHs) that relies on the controlled generation of transient heterocyclic alkynes and arynes. The strained intermediates undergo in situ trapping with readily accessible oxadiazinones. Four sequential pericyclic reactions occur, namely two Diels–Alder / retro-Diels–Alder sequences, which can be performed in a stepwise or one-pot fashion to assemble four new carbon–carbon (C–C) bonds.

A Vicinal Electrophilic Diborylation Reaction Furnishes Doubly Boron-Doped Polycyclic Aromatic Hydrocarbons

2017 ◽  
Vol 56 (20) ◽  
pp. 5588-5592 ◽  
Author(s):  
Alexandra John ◽  
Michael Bolte ◽  
Hans-Wolfram Lerner ◽  
Matthias Wagner
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Aromatic Hydrocarbons ◽  
Boron Doped ◽  
Polycyclic Aromatic

Cyclic Alkyne Approach to Heteroatom-Containing Polycyclic Aromatic Hydrocarbon Scaffolds

2019 ◽  
Author(s):  
Evan Darzi ◽  
Joyann Barber ◽  
Neil Garg
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Polycyclic Aromatic Hydrocarbon ◽  
Aromatic Hydrocarbon ◽  
Aromatic Hydrocarbons ◽  
Diels Alder ◽  
Pericyclic Reactions ◽  
One Pot ◽  
Synthetic Strategy ◽  
Polycyclic Aromatic

We report a modular synthetic strategy for accessing heteroatom-containing polycyclic aromatic hydrocarbons (PAHs) that relies on the controlled generation of transient heterocyclic alkynes and arynes. The strained intermediates undergo in situ trapping with readily accessible oxadiazinones. Four sequential pericyclic reactions occur, namely two Diels–Alder / retro-Diels–Alder sequences, which can be performed in a stepwise or one-pot fashion to assemble four new carbon–carbon (C–C) bonds.

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